Ben-Izhak O, Itin L, Feuchtwanger Z, Lifschitz-Mercer B, Czernobilsky B
Department of Pathology, Rambam Medical Center, Haifa, Israel.
Int J Surg Pathol. 2001 Jul;9(3):249-53. doi: 10.1177/106689690100900314.
Calcifying fibrous pseudotumor (CFP) is a benign soft tissue lesion composed of thick collagen bundles, scattered fibroblasts, and psammomatous and dystrophic calcifications, located most commonly in the extremities and trunk of children and young adults. The present case in a 36-year-old woman is to the best of our knowledge the first report of a large CFP confined to the mesentery, which, because of torsion, led to acute peritonitis and emergency laparotomy. The typical histologic features were accompanied by a prominent myofibroblastic proliferation along with inflammatory response at the periphery of the lesion. The spindle cells of the lesion were positive for vimentin and focally for CD34 and smooth-muscle actin. Review of the literature and discussion of differential diagnosis in this report focuses on abdominal CFP and other intraabdominal soft tissue lesions, some of which may be precursors of CFP. Int J Surg Pathol 9(3):249-253, 2001
钙化性纤维性假瘤(CFP)是一种良性软组织病变,由粗大的胶原束、散在的成纤维细胞以及砂粒体样和营养不良性钙化组成,最常见于儿童和青年的四肢及躯干。据我们所知,本病例为一名36岁女性,是首例局限于肠系膜的巨大CFP报告,该病变因扭转导致急性腹膜炎并进行了急诊剖腹手术。典型的组织学特征伴有病变周边明显的肌成纤维细胞增生及炎症反应。病变的梭形细胞波形蛋白阳性,部分CD34和平滑肌肌动蛋白阳性。本报告中对文献的回顾及鉴别诊断的讨论聚焦于腹部CFP及其他腹腔内软组织病变,其中一些可能是CFP的前驱病变。《国际外科病理学杂志》9(3):249 - 253, 2001